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PRAVASTATIN SODIUM

NDC 55154-7998 · Cardinal Health 107, LLC

Generic namePRAVASTATIN SODIUM
Dosage formTABLET
RouteORAL
Active ingredient(s)PRAVASTATIN SODIUM
Strength40 mg/1
Pharmacologic classHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Marketing categoryANDA

Packages

55154-7998-0 — 10 BLISTER PACK in 1 BAG (55154-7998-0) / 1 TABLET in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51655-594 — Pravastatin Sodium, 51655-708 — PRAVASTATIN SODIUM, 51655-976 — PRAVASTATIN SODIUM, 55111-229 — Pravastatin sodium, 55111-230 — Pravastatin sodium, 55111-231 — Pravastatin sodium, 55111-274 — Pravastatin sodium, 55154-3350 — PRAVASTATIN SODIUM, 55154-5370 — Pravastatin Sodium, 55154-7275 — PRAVASTATIN SODIUM, 55700-994 — Pravastatin Sodium, 60505-0168 — PRAVASTATIN SODIUM, 60505-0169 — PRAVASTATIN SODIUM, 60505-0170 — PRAVASTATIN SODIUM, 60505-1323 — PRAVASTATIN SODIUM, 60687-178 — Pravastatin Sodium, 60687-886 — PRAVASTATIN SODIUM, 60687-897 — PRAVASTATIN SODIUM, 60687-908 — PRAVASTATIN SODIUM, 61919-708 — Pravastatin Sodium, +170 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.